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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does FLOVENT Cause Product quality issue? 8 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 8 reports of Product quality issue have been filed in association with FLOVENT. This represents 8.3% of all adverse event reports for FLOVENT.

8
Reports of Product quality issue with FLOVENT
8.3%
of all FLOVENT reports
0
Deaths
5
Hospitalizations

How Dangerous Is Product quality issue From FLOVENT?

Of the 8 reports, 5 (62.5%) required hospitalization.

Is Product quality issue Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for FLOVENT. However, 8 reports have been filed with the FAERS database.

What Other Side Effects Does FLOVENT Cause?

Dyspnoea (24) Asthma (13) Drug ineffective (13) Cough (11) Malaise (10) Fatigue (9) Chronic obstructive pulmonary disease (8) Investigation (8) Pneumonia (8) Drug administration error (7)

What Other Drugs Cause Product quality issue?

ETONOGESTREL (4,651) ALBUTEROL (4,466) TIOTROPIUM (3,821) MOMETASONE FUROATE (3,406) LIDOCAINE (3,126) FLUTICASONE\SALMETEROL (2,986) FORMOTEROL\MOMETASONE FUROATE (2,458) FENTANYL (2,450) NICOTINE (1,987) EXENATIDE (1,839)

Related Pages

FLOVENT Full Profile All Product quality issue Reports All Drugs Causing Product quality issue FLOVENT Demographics